Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Executive-IPQA Date: Jun 5, 2025 Location: Mohali - Quality Control Company: Sun Pharmaceutical Industries Ltd Ensure compliance to cGMP for all operational activities. Monitor the formulated products against stipulated conditions mentioned in the Batch production record. Conduct certificate of batch production records for compliance and stage wise completion. Conduct line clearance during manufacturing and the packing activities. Conduct sampling activities during the manufacturing and the packing activities. Conduct qualification, PPV, PM and calibration of in-process instruments as per schedule. Swab and Rinse sampling activity for cleaning validation and verification studies. Initiate Deviation, Change Control and Investigations. Provide support to conduct investigations related to deviation, CAPA, OOS, OOT, and Market complaint handling. Issuance of Batch production records. Review & Verification of Bin for Documents / Labels Destruction as per SOP. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Manager - QA Date: May 11, 2025 Location: Guwahati - Quality Assurance Company: Sun Pharma Laboratories Ltd Job Summary: The position is responsible for heading the Quality Assurance function in NOSD Parenteral Block at Sun Pharma laboratories Limited, Guwahati Responsible to set the team goals and objectives for the NOSD Quality at Guwahati site in alignment with goals of Cluster Quality and other business function(s). Responsible to collaborate and support to functional heads of QA, QC, Microbiology, Production, IT, Regulatory Affairs and commercial department to align organizational goal and business strategies for achieving overall quality. Responsible for providing guidance to ensure achievement of targeted completion of tasks and execution of team. Responsible for facilitate harmonization and consistent implementation or Quality Systems and procedures (Pertaining to parenteral), in alignment with Global Quality Policies, Standards and applicable SOPs. Essential Job Functions: Primary Responsibility: Review and monitoring of Quality operations at Parenteral Block. To execute, monitor, review, and approval of Quality management systems i.e. Change control, Deviation, and CAPA management as per requirements. To review and approve Standard Operating Procedure etc. To ensure the compliance of documentation at various stages of the process i.e. (Manufacturing, Filtration, Filling, Visual Inspection, Labelling and Packing operations). To review, approve the Master and executed BMR, BPR, Validation, Qualification and other GMP documents. To evaluate and monitor the Aseptic process simulation (Media Fill) activities with respect to the APS planner, Trending of intervention protocol & reports. To facilitate harmonization and consistent implementation of the quality systems and procedures at the site in alignment with corporate quality policies /procedures. To review, update, respond to GQS/Regulatory audit observations within the stipulated time frame. To participate in the review & approval of investigation in case of Non- conformance events i.e. Process Deviation, OOS, OOT & Product Quality Complaint. To ensure release, approval, or rejection of Raw Material, Packing Material, Intermediate, Finished products as per approved specifications. To ensure completion and implementation of CAPA as per established procedure and follow up to verify the effectiveness of CAPA. Responsible for the batch disposition (Batch release or reject). To ensure compliance of electronic systems such as manufacturing equipment/instruments etc. To ensure equipment /instrument, qualification/calibration and prevent maintenance are performed as per approved planner. To ensure that processing and storage area are qualified as per the approved procedure and GMP requirements. To impart training to the plant personnel as per requirement and ensure the effectiveness. To be part of self-inspection and or quality audits that regulatory appraises the effectiveness and applicability of the quality system as per schedule. To ensure and perform work as per established approved procedure, regulatory norms and its compliance as per the current regulatory requirement. Facilitate/support the implementation of new initiatives of Corporate functions at site. Secondary Responsibility Specific emerging projects as applicable. Perform any other responsibility assigned by the Quality Head/Management. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: General Manager Production Date: May 30, 2025 Location: Paonta Sahib - Plant Company: Sun Pharmaceutical Industries Ltd Job Role : Production Head Job Grade : General Manager (G7) Location : Paonta Job Responsibilities: To ensure delivery of products in time, of desired quality and quantity at optimum cost. Commit to Demand & Supply to commit as per Key Performance Indicator targets. To ensure continuous improvement in achievement of productivity, manufacturing yields & quality norms; Launch of new products 100% in time. Quality: Demonstrate compliance to established Manufacturing Operations and Quality Standards. To ensure that products are produced and stored according to the appropriate documentation in order to obtain the required quality. Strive for reduction in Out of Specification, Deviations, reduce Market complaints. Document Integrity: To support compliance of practices to established procedures and Good Manufacturing Practice standards. To approve the SOPs & format, batch records relating to production operations and to ensure their strict implementation. Cost: Overhead recovery, and manufacturing efficiency to be maintained. Cascading Sun Values and culture to the root level. People Development: Develop Talent pipelines for level Il, Ill & IV key jobs. Monitoring and control of the manufacturing environment; Process validation and calibration of analytical apparatus; Designation and monitoring of storage conditions for materials and products; compliance with GMP requirements; To ensure the qualification and maintenance of department, premises and equipment. To ensure that the appropriate validations are done. Retention of records; Performance and evaluation of in-process controls; Training, including the application and principles of QA; To design and implement the policies, systems and procedures as required for the efficient management of the shop floor. To co-ordinate with other departments to control costs to meet the business goal. To plan for budgetary expenses and control them. To enhance the productivity by working on different projects. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Hi, we expecting candidate within Tamil Nadu and must Experience in Manufacturing Industry / Chemical Processing /Pharma/ FMCG Industry/sugar industry. Qualifications: A bachelor's degree in Electrical and Instrumentation Engineering, electrical engineering, or a related field is typically required. 4-5 years hands on FMCG Industry/chemical industry etc., Manufacturing plant experience in instrument engineering. Knowledge of DCS/PLC/SCADA Having knowledge in, maintaining control systems. Conducting calibration, testing and maintenance of systems. Ensuring instruments adhere to health, safety and legal regulations. The Instrument Engineer is responsible for maintenance of the instrumentation for all plant operations, including field installations and associated control devices responsible for developing maintenance and reliability related to the instrumentation. Responsibilities: Provides technical support for the maintenance, operation, and troubleshooting of the plant's instrumentation systems and equipment, including low voltage electrical systems, Distributed Control System and machinery controls and ensure proper maintenance of the same. Investigates instrumentation equipment failures and recommends actions to enhance the system and equipment reliability. Benefits: subsidiary Food provided Health insurance Paid time off Provident Fund Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Sr. Executive - QA Date: Jun 6, 2025 Location: Jammu - Quality Assurance Company: Sun Pharma Laboratories Ltd To Prepare, manage and review validation master plan and cleaning validation master plan. To prepare and summarize results when writing final validation. To review and coordinate for all type of third party calibration. To prepare execute protocols and report of process validation, hold time study, HVAC, Water system and collection of samples. To initiate and evaluate of change control, risk assessment of product as well as equipment. To prepare annual product review and provide data related to validation and qualification. To follow and implement current GDP and SOP during work. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Executive Date: May 23, 2025 Location: Jammu - Operations Company: Sun Pharma Laboratories Ltd To ensure proper receipt of packing material & misc material after proper verification of documentation, preparation of GRN. To ensure proper verification and segregation of material before preparation of GRN. To ensure material is stored as per locator codes. To ensure proper issuance of packing material from production department. To ensure proper returns of issued packing material from production department. To ensure proper maintenance of documents and records. To prepare MDN's as per SOP as & when required. To ensure day to day records of humidity / tempreture/ performance of weighing scales is being carried out and recorded. To ensure proper handling of rejected material as per SOP. To ensure proper disposal of scrap as and when rquired. To ensure timely release of packing material for production. To generate requirement of packing material and place purchase requisition as per RFC. To follow Trackwise, EDMS for change controls and revision of SOP's as and when required. To maintain the records for calibration, validation of all the equipments installed in warehouse. To reconcile all packing materials as and when required and maintain proper locator codes. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Manager - Engineering & Projects Date: May 29, 2025 Location: Dewas SGO - Engineering Block P Company: Sun Pharmaceutical Industries Ltd Job Description Position: Engineering Penem Head Department: Engineering and Projects Designation: Senior Manager – II Total Years of Experience: 15+ Years Education Qualification: B.E. in Electronics Job Role: Accountable for Engineering and Maintenance related activities for Block P (Sterile), Block F (OSD), Supporting Facilities (Micro/Stability, QC, Warehouse and Export Warehouse) and External area. Site Projects, Process Control System (PCS) Validation and Support to IT Compliance. Responsibilities: Overall responsible and accountable for engineering and maintenance related activities of Block P (Sterile), Block F (OSD), Supporting Facilities (Micro/Stability, QC, Warehouse and Export Warehouse). Overall responsible and accountable for upkeep of external facility of site. Maintain the expense (Power/ Fuel/ Water/ Spares/ R&M) within the budget. Review and effectively implementation of Preventive Maintenance, Facility Maintenance and Calibration System. Promptly attend the maintenance related work of equipment’s/ system/ Facility to minimize the losses. Analysis of plant breakdowns, and initiate corrective measures for prevention, maintain MTTR within the specified limit. Maintain the HVAC; maintain the environmental condition in the manufacturing area as per specifications. Site Project and Site upkeep project management. Prepare Monthly Engineering Update for SGO. Spare requirement assessment and procurement initiation. Continuous evaluation/ maintenance of engineering equipment/ facility. Engineering drawing management. Vendor bill approval, GRN Verification. Ensure compliance to engineering regulatory requirement in the manufacturing. Ensure implementation and Compliance of SOPs. Ensure data integrity visibility at workplace. Extend support in qualification and Validation. Manage the Process Control System Validation activities at site. Provide support to IT Compliance. CAPA, Deviation and Change Control Management of Engineering Department. Maintain the safe working condition in the area and compliance to EHS SOPs. CSP development and assessment. Provide support to Scrap Management. Educating and trained to all the engineering persons including engineering CSPs for compliance. To ensure contamination control are available and followed at site as per Contamination Control Strategy (CCS) and respective procedures. People Development – Knowledge sharing with team to improve the technical competency level. Time to time guidance to subordinate for proper planning and excel the individual and team performance. Motivate the team and develop team spirit among the departmental people. SME Management, represent engineering department during various inspections. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Head Microbiology Date: May 16, 2025 Location: Dewas SGO - Plant Company: Sun Pharmaceutical Industries Ltd JOB DESCRIPTION Position : Microbiology Head Reports to: Quality Head Department: Quality Grade: G8 Functional Area: QC - Microbiology Location: Dewas POSITION SUMMARY Manage overall site microbiology department wrt sampling, testing, planning, qualifications, media fill program ( for sterile manufacturing),compliance and upgrades of facilities and procedures. Conduct effective review of team and portfolio, provide direction and guidance to the team and develop team competence with the objective of ensuring the quality of products released with adherence to GMP norms and timelines The incumbent will assure individual compliance with the all concerned regulatory requirements, GxP’s and applicable department programs, including training, documentation, Standard and Procedures. Key Responsibilities: Provide leadership and direction to achieve all quality goals. Manage & Organize timely microbiological sampling, testing and release of raw materials, finished product, commercial stability, Exhibit stability, miscellaneous samples. Manage & Organize timely Microbiological sampling, testing and release of water and Utility samples. Manage & Organize timely Microbial Environmental Monitoring of passive air/active air/ Compressed air/equipment surfaces /personnel monitoring & Drain points of manufacturing blocks, warehouses & Microbiology lab etc. Monitoring effectiveness of the disinfectants used at the site and make appropriate timely change to the ineffective proved disinfectants. Manage & Organize timely handling & maintenance of microbial cultures. Isolation & identification of microbial isolates from various sources. Manage & Organize timely laboratory investigation of out of specification results /Out of trends/Out of limit, root cause analysis and Risk assessment and Health hazard evaluation of identified microorganisms. Participate in internal, external and/or regulatory inspections of Microbiology operations at the site. Learn from external regulatory audit observations and implement Global CAPA and local CQA observations CAPA in micro lab Ensure trend and annual summary reports of water/microbial environmental monitoring/Microbial isolates etc. Ensure calibration, validation and qualification of laboratory equipment/instrument. Ensure timely availability of laboratory Chemicals, media/ stationary/ gloves and Consumable. Ensure consistency in Microbiology lab operations and drive continuous improvements in laboratory performance. Ensure compliance to cGMPs and applicable safety standards in the Microbiology laboratory. Train microbiologist about the microbiological techniques, aseptic practices, critical quality management skills, including decision-making, handling of quality exceptions, staff development, personnel and planning, etc. Managing people on a day-do-day basis. Preparation of annual capex & revenue budget for microbiology section. Ensure adherence to approved budget work plan. Oversee that the cost of testing is controlled in microbiology lab. Liaison with Corporate Micro team to implement microbial risk assessment program and work to mitigate effective CAPA’s to prevent failures. MINIMUM EDUCATION/EXPERIENCE REQUIREMENTS Microbiology Graduateor Equivalent REQUIRED SUCCESS ATTRIBUTE Minimum 15years with Microbiology work experience preferred Knowledge Of GxP’s, CGMP And Other Regulatory Requirements. Compliance Collaboration Accountability Customer service orientation Planning and prioritization Secondary Success Attributes Attention to detail People connect Emotional control Effective communication Problem solving Roles Additional Responsibilities Can Be Assigned As Required. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: QA Sterile Manager Date: May 23, 2025 Location: Dewas SGO - Quality Assurance Company: Sun Pharmaceutical Industries Ltd Job Description Position: QA Sterile Manager Department: Quality Assurance Designation: Manager - I Education Qualification: M.Sc. in Biotechnology / Microbiology / Chemistry Total years of Experience: 10+ Years Job Role: Management of Quality Assurance functions of Manufacturing Block – P. Responsibilities: Ensure that manufacturing and packing of the batch is executed and records are completed and reviewed in accordance with established SOPs and cGMP regulations. Conduct certification of batch production records for compliance and stage-wise completion. To release / reject the Batch after complete review of batch and related quality documentation. Tracking and monitoring of QMS system. Ensure logical closure of deviations and investigations of related product before release. Conduct thorough investigations along with production for any complaints / deviations/ OOS / stability failure for products manufactured at the site and logical / timely closure of Complaints. To ensure contamination controls implemented and followed at site as per contamination controls strategy (CCS) and respective procedures. Work directly with planning, QC, other QA functions, and Regulatory Affairs to ensure Batches are released to meet supply chain requirements. Participate in self-audits of facility and equipment in partnership with Manufacturing and Engineering to ensure readiness for operations. Participate in Aseptic simulation (Media Fill) activity, Monitoring and Implementation for PENEM DF. Identify continuous improvement opportunities to improve compliance, process clarity, and operational efficiency. Review and approve master batch production records (Manufacturing / packing) and SOPs. Review and approve equipment qualification & process validation protocols and reports for accuracy, completeness, and traceability as well as adherence to protocol / procedures. Review and approve Annual Product Review (APR) reports for the products as per the schedule. Stability sample management of finished goods. Management of control sample pertaining to collection, review, storage and destruction. Management of line clearance, in-process check, coding approval and water sampling. Review and approval of IPQA instrument calibration record. Management of IPQA activities for Block-Penem. Review and approve artwork of Packaging material, STP and Specification. Provides appropriate training and development to support staff to meet their respective job responsibilities. Work in partnership with Manufacturing, Engineering, and QC to increase knowledge and understanding of cGMPs and improve practices and procedures. Review activities related to the Microbiology Laboratory. Review activities related to the beta-lactam containment monitoring. Compliance with Quality Policy of the organization. Improvement of System and procedures, Quality of products manufactured and delivered. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Designation: Plant Head Department: Operations Location: Pithampur, Madhya Pradesh Reporting To: CEO Experience Required: 10–20 years in manufacturing (preferably automotive/Forging/Machining or Relevant business domain) Qualification: B.E./Diploma in Mechanical Engineering or related field 🎯 Objective of the Role To lead and manage the entire plant operations including production, quality, maintenance, planning, dispatch, and safety, ensuring optimum productivity, cost-effectiveness, customer satisfaction, and employee engagement. 🛠️ Key Responsibilities 1. Production & Operational Management Oversee daily operations including fabrication, machining, forging, and dispatch. Ensure timely and quality production as per monthly/weekly schedules. Drive OEE (Overall Equipment Effectiveness), reduce downtime, and improve throughput. 2. Manpower & Team Leadership Lead a team of Production Managers, Quality Heads, Maintenance, Stores, HR, and Supervisors. Ensure discipline, skill development, and motivation across all levels. Implement shift planning and manpower allocation. 3. Planning & Inventory Control Coordinate with PPC and stores to ensure raw material availability and inventory control. Minimize wastage and monitor rejections, scrap, and rework. 4. Quality & Compliance Ensure adherence to customer quality standards (PPAP, APQP, ISO/TS 16949). Conduct internal audits and quality improvement drives. Ensure traceability, calibration, and process control. 5. Maintenance & Tooling Monitor preventive and breakdown maintenance. Oversee availability of critical spares and die/tool maintenance. 6. Cost Control & Efficiency Drive cost reduction initiatives in manufacturing, energy, and manpower. Optimize machine utilization, shop floor layout, and takt time. 7. Health, Safety & Environment Ensure safe working conditions and compliance with EHS norms. Conduct safety drills, audits, and safety committee reviews. 8. Customer Coordination Act as the single point of contact for production, quality, and delivery concerns. Handle customer visits, audits, and emergency escalations. 9. MIS & Reporting Present daily, weekly, and monthly dashboards to management. Review KPIs such as Production Output, Rejections, Downtime, and Delivery OTIF. 📊 Key Performance Indicators (KPIs) Production Efficiency (Planned vs. Actual Output) On-Time Delivery (OTD) Customer Complaint Rate Downtime % Scrap & Rework Rate Cost per Unit Employee Turnover and Engagement 🤝 Skills & Competencies Strong leadership and team management skills Hands-on in manufacturing systems (Lean, 5S, Kaizen) Conflict resolution and cross-functional coordination Proficiency in MS Excel, ERP, and Production software Analytical, disciplined, and goal-oriented mindset Show more Show less

Long Description WHO WE ARE AVI-SPL is a digital enablement solutions provider who transforms how people and technology connect to elevate experiences, create new value, and enable organizations to thrive and grow. We are the largest provider of collaboration technology solutions, which include our award-winning managed services. Our highly certified industry experts and innovation leaders share a vision to help people work smarter and live better. We believe that success starts with a sound team and that an inclusive and diverse workplace moves us all forward. Essential Duties And Responsibilities Develop and generate all necessary drawings for integrated AVI-SPL customer projects Coordinate with Design Engineers, Project Engineers and Project Managers to complete drawings accurately and timely Provide high-level customer service to internal and external customers daily Research components as needed to create an accurate depiction Act as customer liaison in absence of the Senior CAD Technician Utilize and test calibration of equipment Responsible for contributing to job documentation as needed Assist with projector and Screen Support Structure installations Operate small and large scale office printers/plotters Utilize labeling software for rack and field wiring purposes Skills And Abilities Proven proficiency in AutoDesk AutoCAD Ability to read and interpret electronic schematics and architectural blueprints Ability to successfully handle multiple projects simultaneously Knowledge of signal flow for audio, video and control systems Understanding of site survey’s Familiarity of Audio Visual, Mechanical, and Electrical facilities drawings. PC proficient Education And/or Experience Minimum High school diploma or equivalent Minimum of 1 year CAD experience preferred 1 year of customer interaction experience preferred E More About Us AVI-SPL is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, protected veteran status, disability status, or membership in any other group protected by federal, state, or local law. AVI-SPL reserves the right to alter work hours and work location as necessary. Work hours may vary based on client requirements and may include travel to various locations in support of the account. Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Manager 2 Date: May 15, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Development & Qualification of multiplex based cytokine release assay and Elispot/ flow cytometry based T cell assays to measure the innate and adaptive Immunogenicity of synthetic peptide products Job Responsibilities: Manage the study sample analysis for pipeline products, preparation of study schedule, design of experiments, trouble shooting, data analysis and review of reports. Isolation of PBMC from whole blood and maintenance of commercial cell lines. Coordinate with internal and external stakeholders for reagent procurement, blood collection, instrument installation and calibration. Statistical analysis of data using software. Preparation/ review of standard operating procedures (SOP), method development reports (MDR), sample analysis report (SAR) and analytical test procedures (ATP). Responsible for operating and maintaining analytical laboratory in compliance with GLP regulations. Responsible for the operation and maintenance of the Flow Cytometry, Multiplex, ELISPOT and other instruments and statistical software. Managing of chemicals, consumables & critical reagents inventory. Performing calibration of instruments and equipment. Troubleshooting instrument performance and equipment issues. Draft responses for regulatory queries and facilitate internal and external audits. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Executive Date: May 18, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Primary Responsibilities: Analytical Method development for API/NCE sample. Analysis of raw material, Intermediate, API/NCE samples on gas chromatography, liquid chromatography and chemical analysis. Method validation for API/NCE purity, impurity, excipients methods. Trouble shooting of various analytical issues for various products. Maintenance, calibration & trouble shooting of HPLC and GC. Preparation of SOP for related to instrument and system. Method transfer and method demonstration at other location as and when required. Documentation like ATP, Development report, Validation protocol, Validation report, STP preparation. To work as per cGMP/OECD GLP and to ensure its compliance. Basic understanding of ICH guidelines Candidate should have basic knowledge about handling of instruments like UV visible spectrophotometer High-performance liquid chromatography Ultra-performance liquid chromatography Karl-Fischer Titration Differential scanning calorimetry USP Dissolution Apparatus I and II Other minor equipment like analytical balance, pH meter, Sonicator and microcentrifuge. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Executive - Analytical Development Date: May 22, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd To work as per cGMP and ensure its compliance as per current guideline and SOPs. Responsible to take training before execution of allotted work & maintaining the training file. Responsible to follow safety precaution as per laboratory procedure. Responsible to escalate any issue / incident to reporting manager for prompt corrective action. Responsible for method development studies for various finished products. Responsible for method Validation studies for various finished products. Responsible for routine and stability studies of various finished products. Responsible to align with organization goal. Other responsibilities assigned by reporting authority. Responsible to follow Quality Management Document procedure. Responsible to perform the calibration of instrument. Responsible to prepare Study Protocol and Study Reports. Responsible to maintain instrument/equipment as per SOPs. Responsible for timely archival of documents as per SOP. Responsible to follow safety precaution as per laboratory procedure. Responsible to ensure proper Handling and Disposal of waste. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Manager - 1 Date: May 21, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Characterization of RLD pack samples. Finalization of packing configuration for Exhibit batch packing of new generic product/NDA as per requirement. Identification of new packaging material & new vendor development for packaging materials. Mold development for primary packaging material & secondary packaging material & its validation. Support to Regulatory team on ANDA’s/NDA’s filling for regulated market. Coordination with NPI & planning team for launch of ANDA’s/NDA’s. Preparation & revision of packaging material specification. Preparation & review of MPC, FMEA, TA, DHF & AFMEA. Preparation & review of Development Study protocol & report & execute the study. Performing functional test as per regulatory requirement. Coordination with Cross functional team like (FDD/RA/Plant/Marketing/PMO) for completion of task. Participating in FAT of machines. Support to plant for validation, trouble shooting and market complaints. SOP preparation, periodic review and packaging lab equipment handling/maintain calibration records. Preparation of Packaging documentation (Pack Style, Justification Report etc. as per Product/Regulatory) as required. Handling of primary and secondary packaging material in storage area & maintaining the PM quantity for stability packaging at R&D. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Sr.Officer LIMS (Master Data Reviewer) Date: May 30, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Job Responsibilities: JOB DESCRIPTION- LIMS Masterdata Reviewer (Sr. Officer) To have thorough knowledge and understanding of QC workflows (Analysis/ Review/ Approve/ Investigation etc.), Analytical methods (Instrumental/ Pharmacopoeial chapters/ Monographs), QC instrumentation activities (operation, calibration, preventive maintenance etc.) and Analytical method validation/Method transfer activities and other processes of QC. To have thorough knowledge and understanding of Analysis reporting requirements of all stages of product for eg, but not limited to; Finished product, API, Excipients, Process validation, Hold time, Swab/rinse samples, Stability including result reporting, trending, COA requirements etc. To support for timely execution and completion of Masterdata activities. To ensure Masterdata creation and review as per established procedures and ensure updation of masterdata as per the observations, if any. To list down observations for any discrepancies found during creation/review of masterdata and share to respective team for resolution. To handover reviewed Masterdata for further process and keep track of closure of observations, if any. To track Masterdata activity status for creation, review and observation closure etc. To coordinate masterdata change management to ensure ongoing compliance with business and regulatory requirements. To have good hands on MS office (i.e. Word / Excel / Power Point) and other computer skills Education Qualification : M.Sc / B.Sc / B.Pharm Experience - 5 To 6 Yrs Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Executive Date: May 29, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd GLP Bioanalytical To Access Study Plan and Standard Operating Procedures and to comply with instructions given in Study Plan and Standard Operating Procedures. To record raw data promptly and accurately and in compliance with the Principles of Good Laboratory Practice, review of raw data and are responsible for the quality of their data. Operation Maintenance and Calibration of Liquid Chromatography and Tandem Mass Spectrometer (LC/MS/MS). To perform the method Development, method validation and study sample analysis (non-clinical) for GLP Studies. Preparation of ATP (Method SOP), SOPs, Template for GLP Studies. Sample preparation for MD, MV and study analysis as per GLP guidelines. Pipette Maintenance and calibration assigned to the group. Other Job Responsibilities Assigned By Reporting Authority. Preparation of method validation/partial method validation reports and bioanalytical study reports for GLP studies in consultation with Study Director/Principal Investigator and in compliance with the Principles of GLP. Documentation of any type of Deviation in GLP study report & communicated directly to the Study Director and/or if appropriate, the Principal Investigator. Responding to QA observations for bioanalytical reports in consultation with Study Director/Principal Investigator and in compliance with the Principles of GLP. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Executive Date: May 10, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Primary Responsibilities: Analytical Method development for API/NCE sample. Analysis of raw material, Intermediate, API/NCE samples on gas chromatography, liquid chromatography and chemical analysis. Method validation for API/NCE purity, impurity, excipients methods. Trouble shooting of various analytical issues for various products. Maintenance, calibration & trouble shooting of HPLC and GC. Preparation of SOP for related to instrument and system. Method transfer and method demonstration at other location as and when required. Documentation like ATP, Development report, Validation protocol, Validation report, STP preparation. To work as per cGMP/OECD GLP and to ensure its compliance. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Executive Biotechnology Date: May 28, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd The candidate is expected to develop Surface Plasmon Resonance (SPR) based methods to measure the kinetic and equilibrium binding constants for protein and peptide products. Responsible for analytical method qualification for all pipeline products. Characterization of innovator product batches sourced from different geographical region and preparation of quality target profile. Analytical similarity assessment of in-house products. Preparation of method development reports (MDR) and analytical test procedures (ATP). Responsible for operating and maintaining analytical laboratory in compliance with GLP regulations. The candidate is responsible for the operation and maintenance of the SPR instruments To manage chemicals,consumables & critical reagents inventory. Performs calibration of instruments and equipment. Troubleshoots instrument performance and equipment issues. Educational Qualification: M.SC./ in Biochemistry / Life Sciences / Biotechnology. Technical/functional Skills: Sound knowledge of analytical method development, qualification and structural and functional characterization of therapeutic proteins. Experience of biosimilarity assessment of biologics for regulated market is desirable. Experience of analytical development for monoclonal antibodies and peptide is highly desirable. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Job Title: Head of Maintenance & Engineering Location : Sunrise Hospital Pala - Ponkunnam Rd, Kaduvamuzhi, Erattupetta, Kerala 686121 Department: Engineering & Maintenance Employment Type : Full-Time Number of vacancies : 1 Qualification & Requirements : Bachelor’s degree in Mechanical/Electrical/Civil Engineering (B.E./B.Tech). 3 years of experience in engineering and maintenance roles, preferably with 2 years in a hospital or healthcare setting. Strong understanding of hospital facility management, medical gases, HVAC, BMS (Building Management Systems), and firefighting systems. Knowledge of healthcare compliance standards (NABH, JCI, local municipal and fire codes). Proven leadership, planning, and troubleshooting abilities. key Responsibilities Facility & Infrastructure Management Oversee maintenance of hospital buildings, wards, labs, ICUs, OTs, emergency units, and support services. Ensure proper functioning of HVAC, electrical systems, plumbing, elevators, and backup power (generators, UPS). Supervise preventive and corrective maintenance schedules. Biomedical & Equipment Oversight Coordinate maintenance and calibration of medical equipment in collaboration with the Biomedical Engineering team. Ensure timely servicing and minimal downtime of all critical medical devices. Compliance & Safety Ensure adherence to local, state, and national safety codes and hospital regulations (e.g., NABH, fire safety, pollution control board). Manage regular inspections, audits, and certifications of engineering systems. Lead emergency preparedness for engineering-related contingencies (fire drills, power failures, etc.). Vendor & Project Management Supervise contractors, service providers, and vendors for AMC contracts, repairs, and facility upgrades. Evaluate and manage facility improvement or expansion projects, including budgeting and execution. Team Leadership Lead and develop a team of engineers, technicians, electricians, plumbers, and support staff. Provide training and SOPs for engineering staff to maintain high performance and safety standards. Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹45,000.00 per month Schedule: Rotational shift Work Location: In person

Our vision is to transform how the world uses information to enrich life for all . Micron Technology is a world leader in innovating memory and storage solutions that accelerate the transformation of information into intelligence, inspiring the world to learn, communicate and advance faster than ever. Facilities Control Technician Roles & Responsibilities As the Micron Facilities Control Technician, you are required to perform maintenance and support engineering works in the fields of Control equipment and system on site, with the necessary guidance and direction from Facilities organization, to achieve facilities department, site, facilities corporate and company goals. Responsibilities And Tasks Adhere to company’s environmental safety health policy and procedure, standard operating procedure with risk assessment, good housekeeping standard and quality policy when performing work. Plan, schedule and perform Preventive and Corrective Maintenance work activities on controls equipment, Gas detection equipment, CCTV, Fire Alarm equipment and system under the responsibilities of Facilities organization. Attend troubleshooting of system abnormalities and assist or lead system recovery. Participate in controls equipment and system abnormalities root cause analysis, then execute corrective and preventive action for continual improvement, this includes installation and modification work on existing or new instrumentation and controls system. Evaluate continuous improvement for preventive maintenance programs. Utilize computer base software to document and analyses records of maintenance work order, equipment history and project tracking. Maintain equipment and system maintenance record for work history traceability. Track and monitor equipment spare parts and consumable inventory. Provide feedback on detail design concept and specifications for installation of new capital equipment and/or system expansion project. Site supervision for installation of new equipment and/or system expansion project at critical milestone during construction phase. Coordinate, sponsor and supervise contract service provider to performance work activities in accordance to defined scope of work and system requirement. Enforce to company’s environmental safety health policy and procedure, standard operating procedure with risk assessment, good housekeeping standard and quality policy when performing work. Job Requirements Diploma in Instrumentation/Control engineering or equivalent related field or experience is preferred. 5-7 years of experience in Semiconductor, Electronics, Pharma or similar kind of manufacturing industries. Detailed and in-depth understanding of facility Instruments/Gas detector/ Variable Speed Drive/ Fire alarm system and its associated system working principle. Good understand of Electrical equipment and PLC wiring concept and its interfacing with Instruments and gas detectors. Execute preventive and corrective maintenance programs for plant instrumentation/gas detection. Good knowledge on the calibration and measurement tools Basic PLC programming knowledge for modification and troubleshooting. Understand system schematic drawings and wiring diagram. Able to work with respective contractor to complete PM jobs effectively. Perform advanced troubleshooting and rectification work independently. Ability to work in a team environment with various professional level. About Micron Technology, Inc. We are an industry leader in innovative memory and storage solutions transforming how the world uses information to enrich life for all . With a relentless focus on our customers, technology leadership, and manufacturing and operational excellence, Micron delivers a rich portfolio of high-performance DRAM, NAND, and NOR memory and storage products through our Micron® and Crucial® brands. Every day, the innovations that our people create fuel the data economy, enabling advances in artificial intelligence and 5G applications that unleash opportunities — from the data center to the intelligent edge and across the client and mobile user experience. To learn more, please visit micron.com/careers All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. To request assistance with the application process and/or for reasonable accommodations, please contact hrsupport_india@micron.com Micron Prohibits the use of child labor and complies with all applicable laws, rules, regulations, and other international and industry labor standards. Micron does not charge candidates any recruitment fees or unlawfully collect any other payment from candidates as consideration for their employment with Micron. Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: QA Head API Date: May 15, 2025 Location: Panoli - Quality Assurance Company: Sun Pharmaceutical Industries Ltd JOB DESCRIPTION Position : QA Head Effective Date: Reports to : Quality Head Job Code: Department: Quality Grade: Functional Area: QA Location: Panoli POSITION SUMMARY Manage overall quality assurance oversight and site activities wrt to quality systems: documentation review and SOP update, in-process quality assurance, sampling and batch release, preventive maintenance/calibration/qualification/validation, internal audit, compliance, quality oversight of electronic systems, budget, and continuous improvement of quality systems, RA support, monitoring of pest control, retention sample management as per Good Manufacturing Practices requirements. The incumbent will assure individual compliance with the all concerned regulatory requirements, GxP’s and applicable department programs, including training, documentation, standard operating procedures, and Sun Pharma policies and procedures. Key Responsibilities: Responsible for defining operational strategy and road map for quality assurance management at site. Define site quality assurance goals and strategy in line with Sun Pharma compliance, product quality management objectives and regulatory requirements. Effectively manage the site Quality Assurance activities and resources necessary to smoothly run the QA operation at site. Provide strong leadership and expertise to ensure achievement of all Quality Assurance accountabilities at site. Identify and implement solution for improving existing site quality assurance systems and processes. Coach and develop both direct and, as appropriate, indirect reports through ongoing, example-based performance feedback, annual performance reviews and the provision of training and development opportunities. Ensure that performance issues are managed in a consistent and timely manner. Develop site quality assurance revenue and capital budgets and headcount projections, track and manage expenditures and headcount to budget over the fiscal year. Responsible for ensuring availability of adequate resources, including manpower to maintain compliance with GXP requirements. Assure all time readiness of site for regulatory agency inspections\internal audits and appropriate implementation of corrective actions regarding observations made by the agencies\internal audit teams. Responsible for executing Quality Management Reviews at site, monitor individual Performance and set improvement areas. Responsible for ensuring market complaints, failures, deviations are investigated and corrective and preventive actions are implemented as per set timeline. Responsible for ensuring compliance to regulatory requirements on product, process and release procedures. Ensure release of safe and effective drug products from site as per cGMP requirement and regulatory commitment. Responsible for ensuring smooth collaboration with all Sun Pharma sites and leveraging synergies. Review & tracking of quality assurance metrics e.g. deviation, change control, OOS/OOT, CAPA effectiveness, market complaints with site manufacturing / QC Management and driving them down. Ensure processes for supply chain management / Global Material Sourcing for vendor selection is followed for vendor selection, qualification and monitor vendor quality performance Provide inputs to manufacturing, R&D and PDL work processes to ensure Quality by Design. Accountable for designing/implementing and ensuring compliance to all quality related SOPs, Policies, Standards and QA systems at the site. Facilitate internal and regulatory agency audits, ensuring that findings from site audits are understood, assessed and addressed site wide in a comprehensive manner. Monitor industry trends/issues faced internally and identify scope for improving Site quality assurance management and processes. Responsible for fulfilling all training requirements of quality assurance employees. Ensure the quality policies, standards and procedures for computerized systems are implemented and adhered at site. Ensure all GxP computerized systems are validated in compliance with the quality policies, standards and procedures and are maintained in validated state throughout the lifecycle with adequate security and controls to ensure data security. Review and approve the documents as per quality procedures. Work in partnership with the site cross functions and corporate functions for implementation of new initiatives. MINIMUM EDUCATION/EXPERIENCE REQUIREMENTS Science or Pharmacy Graduate Equivalent 15 years REQUIRED SUCCESS ATTRIBUTE Knowledge of GxP’s, cGMP and other regulatory requirements. Planning and Prioritization Collaboration Accountability Compliance Customer Service orientation Secondary Success Attributes People Connect Attention to detail Emotional control Effective Communication & Problem solving Roles WORKING ENVIRONMENT/PHYSICAL REQUIREMENTS Additional responsibilities can be assigned as required. Incumbent performs work assignments in both normal office and non-aseptic manufacturing/packaging environments. Moderate to loud noise level is common in production rooms. The incumbent must be able to comply with the gowning requirements for entry into controlled non-aseptic manufacturing areas, and wear personal protective equipment as required. DELEGATION OF RESPONSIBILITY In the absence of job holder, delegation of responsibility will be as follows: Upward Delegation – Strategic site responsibilities to higher level Downward Delegation – Operational responsibilities to direct reports or similar job role ___________________ __________ Department Head Date ____________________ __________ Human Resources Date This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job. This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Sr. Manager - Micro Lead Date: Jun 3, 2025 Location: Ahmednagar - Quality Control Company: Sun Pharmaceutical Industries Ltd Job Title: Manager / Sr.Manager – Micro Lead Job Grade: G10 / G9B Function: Global API Business Sub-function: Manager’s Job Title: Skip Level Manager’s Title: Function Head Title: Location: Ahmednagar No. of Direct Reports (if any) Areas of Responsibility To plan, review and monitor overall activities in Microbiology and lead the department. Co-ordination with other departments for priorities and provide the timely support/testing to avoid delay due to analysis. Review of all departmental related documents and review results in LIMS system in microbiology section. Ensure all documents are complete in time. To review the lysate sensitivity test, Bacterial endotoxin test of WFI and API products. To check method validation of bacterial endotoxin test and microbial quality of products. To procure, receipt, storage, maintenance, its use and reconciliation of biological indicator, media, reagents standard cultures and bioball etc. To ensure and check calibration and Operation of TOC analyzer Execute breakdown (If any) in consultation with vender. To ensure environmental monitoring activities performed as per schedule and to check the environmental monitoring reports. To review qualification, Calibration of all instruments in microbiology laboratory as per SOP/Schedule. To participate in investigation and to review of deviations/OOS/OOT/OOC/Lab Event / & review of SOPs as per revision date in micro section online in track wise system. To highlight observations, rejection / failure, quality related concern in time and contribute in troubleshooting To ensure and review all logbooks and registers are maintained on line and available at designated place. Preparation and review of GMP documents related to activities. To review and ensure fumigation activity and its verification as per SOP/Guidelines. To prepare / review trends for water and environment monitoring, Summary report of water and environment monitoring. Responsible to follow online good documentation practices for data recording and monitoring. To ensure and review validation of autoclave, Dry heat sterilizer (DHS), Incubators, Laminar Air flow, HVAC. To ensure and review preparation of reagents and volumetric solution and its standardization as per specification / SOP. To ensure and review inventory and stock record of media/reagents/culture/lysate/CSE/LRW. To ensure to follow the GLP as per current practice in the laboratory. To ensure safety and use of personnel protective equipment’s during day to day activities Responsible for carrying out any other responsibilities assign from time to time orally or in writing by Quality head, however related training imparted to concerns. To support for review and compliance activity in quality function and to support for any time readiness as well as enhancement of system and practices. To Coordinate with corporate functions with respect to microbiology activity. Travel Estimate Job Requirements Educational Qualification M.Sc (Microbiology) Specific Certification Skills Experience 15 to 18 Yrs Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Manager - Production Date: May 19, 2025 Location: Panoli - Prodcution Block 6 Company: Sun Pharmaceutical Industries Ltd Job Description Position: Sr. Manager - Production Job Title: Job Grade: G9A Function: Global API Business Sub-function: Manager’s Job Title: Skip Level Manager’s Title: Function Head Title: Location: Panoli No. of Direct Reports (if any) Areas of Responsibility Production planning and scheduling (day to day basis.) Ensuring resources available (BMR, Raw Material Manpower etc.) Maintain GMP norms and trained the subordinates accordingly. Review the BMR, incident and change control etc. and accordingly co-ordinate with R&D. Co-ordination with Engg. Dept. for preventive maintenance and calibration Ensure to maintain the online documentation and accordingly train the subordinate. Close co-ordination with service dept. like QA, QC, Store, Egg, Safety etc. for Routing work of plant. Ensure create and confirm the process order and ensure to complete the daily entry in SAP HANA. Liaison with QC/QA/Store/Engg. Dept. for solving of trouble shooting problem. Constantly monitoring and improvement of product process, efficiency, services etc. Reporting to higher authority. Ensure Training to subordinate. Ensure Documentation work, monthly reports, data preparation, root cause analysis, incident and change control etc. (process trend analysis). Ensure Preparation/ Revision of BMR & related accessories and SOP. Procurement of consumable items. Actively involves the Process and cleaning validation. (where applicable) Ensuring the Maintaining of documents related to Process/ Cleaning/ HouseKeeping. Control on fresh as well as recovered solvents/ spent solvents Responsible for administrative work related to plant Co-ordination with other department for solid waste, process waste and spent solvent transfer to respective area and record maintaining. To maintain discipline as per company's rules and regulation. Other Activities entrusted from time to time Preparation, review and revision of SOP. Working as a Department Training coordinator in LMS Operation of electronic system like SAP HANA, Leave Portal etc. Travel Estimate Job Scope Internal Interactions (within the organization) External Interactions (outside the organization) Geographical Scope Financial Accountability (cost/revenue with exclusive authority) Job Requirements Educational Qualification MSC / BE/ B.Tech – Chemical Specific Certification Skills API Production Experience 17 to 19 years of work experience. Handle team size of 150 to 200. Handle Production capacity of minimum 50 Cr. In Current role, he should be heading block. Apart from this experience of handling QMS, Capacity Enhancement, Solvent recovery. API regulatory plant experience. 2 | P a g e Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Micro Lead - API Date: May 16, 2025 Location: Ahmednagar - Quality Control Company: Sun Pharmaceutical Industries Ltd Job Description Title: Micro Lead API Location: Ahmednagar Grade: G9B- Sr. Manager 2 JOB RESPONSIBILITIES To plan, review and monitor overall activities in Microbiology and lead the department. Co-ordination with other departments for priorities and provide the timely support/testing to avoid delay due to analysis. Review of all departmental related documents and review results in LIMS system in microbiology section. Ensure all documents are complete in time. To review the lysate sensitivity test, Bacterial endotoxin test of WFI and API products. To check method validation of bacterial endotoxin test and microbial quality of products. To procure, receipt, storage, maintenance, its use and reconciliation of biological indicator, media, reagents standard cultures and bioball etc. To ensure and check calibration and Operation of TOC analyzer Execute breakdown (If any) in consultation with vender. To ensure environmental monitoring activities performed as per schedule and to check the environmental monitoring reports. To review qualification, Calibration of all instruments in microbiology laboratory as per SOP/Schedule. To participate in investigation and to review of deviations/OOS/OOT/OOC/Lab Event / & review of SOPs as per revision date in micro section online in track wise system. To highlight observations, rejection / failure, quality related concern in time and contribute in troubleshooting To ensure and review all logbooks and registers are maintained on line and available at designated place. Preparation and review of GMP documents related to activities. To review and ensure fumigation activity and its verification as per SOP/Guidelines. To prepare / review trends for water and environment monitoring, Summary report of water and environment monitoring. Responsible to follow online good documentation practices for data recording and monitoring. To ensure and review validation of autoclave, Dry heat sterilizer (DHS), Incubators, Laminar Air flow, HVAC. To ensure and review preparation of reagents and volumetric solution and its standardization as per specification / SOP. To ensure and review inventory and stock record of media/reagents/culture/lysate/CSE/LRW. To ensure to follow the GLP as per current practice in the laboratory. To ensure safety and use of personnel protective equipments during day to day activities Responsible for carrying out any other responsibilities assign from time to time orally or in writing by Quality head, however related training imparted to concerns. To support for review and compliance activity in quality function and to support for any time readiness as well as enhancement of system and practices. To Coordinate with corporate functions with respect to microbiology activity. Education : Graduates - Microbiology/ Equivalent ( experience In Micro testing / leading ) Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less